tert-butyl ((4-(3,5-difluorophenyl)tetrahydro-2H-pyran-4-yl)methyl)carbamate

90%

Reagent Code: #195763

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 327.37 g/mol
Formula C₁₇H₂₃F₂NO₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a protected amine intermediate in the synthesis of pharmaceutical compounds, featuring a tert-butyl carbamate (Boc) group. Particularly employed in the development of kinase inhibitors for cancer treatment, where its 4-(3,5-difluorophenyl)tetrahydro-2H-pyran scaffold supports selective binding to enzyme active sites in final drug candidates, enhancing efficacy, metabolic stability, and bioavailability. The Boc protecting group facilitates multi-step medicinal chemistry syntheses by allowing deprotection under mild acidic conditions, enabling easy reaction control and minimizing unwanted side products. Also utilized in research to construct complex molecules and improve water solubility of certain precursors under specific conditions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,580.00
inventory 1g
10-20 days ฿17,110.00

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tert-butyl ((4-(3,5-difluorophenyl)tetrahydro-2H-pyran-4-yl)methyl)carbamate
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Used as a protected amine intermediate in the synthesis of pharmaceutical compounds, featuring a tert-butyl carbamate (Boc) group. Particularly employed in the development of kinase inhibitors for cancer treatment, where its 4-(3,5-difluorophenyl)tetrahydro-2H-pyran scaffold supports selective binding to enzyme active sites in final drug candidates, enhancing efficacy, metabolic stability, and bioavailability. The Boc protecting group facilitates multi-step medicinal chemistry syntheses by allowing depro

Used as a protected amine intermediate in the synthesis of pharmaceutical compounds, featuring a tert-butyl carbamate (Boc) group. Particularly employed in the development of kinase inhibitors for cancer treatment, where its 4-(3,5-difluorophenyl)tetrahydro-2H-pyran scaffold supports selective binding to enzyme active sites in final drug candidates, enhancing efficacy, metabolic stability, and bioavailability. The Boc protecting group facilitates multi-step medicinal chemistry syntheses by allowing deprotection under mild acidic conditions, enabling easy reaction control and minimizing unwanted side products. Also utilized in research to construct complex molecules and improve water solubility of certain precursors under specific conditions.

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